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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504936Generated: October 25, 2026

Triethylamine → 1-Indanone

https://huagongshe.com/reaction/1504936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBinap, (A+-)-HCID 634876—
Reactant1H-inden-1-oneHCID 11815384—
ReactantPhenyl-d5-boronic acidHCID 16213772—
CatalystBis(norbornadiene)rhodium(I) tetrafluoroborateHCID 10915722—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product1-IndanoneHCID 6735—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of compound A (57 g) in tetrahydrofuran (600 mL) was added triethylamine (30 mL) dropwise over 30 min. The reaction mixture was kept at room temperature for 3 hours. The precipitated solid was filtered and the filtrate was concentrated in vacuo. The residue was reprecipitated from diethyl ether to afford compound B (31 g) as a yellow solid. To a solution of compound phenyl-d5-boronic acid (25 g) in 1,4-dioxane/water (900 mL/90 mL) was added [Rh(ndb)2]BF4 (1.3 g), racemic BINAP (2.1 g) and triethylamine (14 mL), then the reaction mixture was kept at room temperature for 2 hours under N2. Then compound indenone (19 g) was added, and the resulting mixture was heated to 100° C. for 3 hours. The precipitated solid was filtered off. The filtrate was concentrated in vacuo. The residue was purified by chromatography to afford indanone C (10 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216961B2
Source datasetuspto-grants-2015_12
ORD IDord-0b1acbdd4a3048dd98572645e4f40659
Source noteuspto-grants-2015_12